Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.67753925C>ACA439930617GNRHRc.411G>T (p.Leu137=)
4g.67753925C>GCA439930618GNRHRc.411G>C (p.Leu137=)
4g.67753925C>TCA439930620GNRHRc.411G>A (p.Leu137=)
dbSNP
4g.67753926A=CA1465420628GNRHRc.410T= (p.Leu137=)
4g.67753926A>CCA357054573GNRHRc.410T>G (p.Leu137Arg)
4g.67753926A>GCA357054575GNRHRc.410T>C (p.Leu137Pro)
dbSNP gnomAD v4
4g.67753926A>TCA357054576GNRHRc.410T>A (p.Leu137Gln)
4g.67753927G>ACA439930625GNRHRc.409C>T (p.Leu137=)
dbSNP
4g.67753927G>CCA357054578GNRHRc.409C>G (p.Leu137Val)
4g.67753927G=CA1465420630GNRHRc.409C= (p.Leu137=)
4g.67753927G>TCA357054579GNRHRc.409C>A (p.Leu137Met)
4g.67753928G>ACA98671975GNRHRc.408C>T (p.Ser136=)
dbSNP gnomAD v4
4g.67753928G>CCA357054581GNRHRc.408C>G (p.Ser136Arg)
gnomAD v4
4g.67753928G=CA1465420636GNRHRc.408C= (p.Ser136=)
4g.67753928G>TCA357054582GNRHRc.408C>A (p.Ser136Arg)
4g.67753929C>ACA357054583GNRHRc.407G>T (p.Ser136Ile)
gnomAD v4
4g.67753929C>GCA357054586GNRHRc.407G>C (p.Ser136Thr)
4g.67753929C>TCA357054585GNRHRc.407G>A (p.Ser136Asn)
4g.67753930T>ACA357054588GNRHRc.406A>T (p.Ser136Cys)
4g.67753930T>CCA357054591GNRHRc.406A>G (p.Ser136Gly)
4g.67753930T>GCA357054589GNRHRc.406A>C (p.Ser136Arg)
4g.67753931G>ACA439930645GNRHRc.405C>T (p.Ile135=)
4g.67753931G>CCA357054592GNRHRc.405C>G (p.Ile135Met)
4g.67753931G>TCA439930648GNRHRc.405C>A (p.Ile135=)
4g.67753932A=CA1465420640GNRHRc.404T= (p.Ile135=)
4g.67753932A>CCA357054594GNRHRc.404T>G (p.Ile135Ser)
4g.67753932A>GCA357054595GNRHRc.404T>C (p.Ile135Thr)
dbSNP
4g.67753932A>TCA357054597GNRHRc.404T>A (p.Ile135Asn)
dbSNP gnomAD v2 gnomAD v4
4g.67753933T>ACA357054599GNRHRc.403A>T (p.Ile135Phe)
4g.67753933T>CCA2938945GNRHRc.403A>G (p.Ile135Val)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.67753933T>GCA357054601GNRHRc.403A>C (p.Ile135Leu)
4g.67753933T=CA1465420642GNRHRc.403A= (p.Ile135=)
4g.67753934C>ACA439930664GNRHRc.402G>T (p.Val134=)
4g.67753934C>GCA439930665GNRHRc.402G>C (p.Val134=)
4g.67753934C>TCA439930666GNRHRc.402G>A (p.Val134=)
4g.67753935A=CA1465420644GNRHRc.401T= (p.Val134=)
4g.67753935A>CCA2938946GNRHRc.401T>G (p.Val134Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.67753935A>GCA357054603GNRHRc.401T>C (p.Val134Ala)
gnomAD v4
4g.67753935A>TCA357054605GNRHRc.401T>A (p.Val134Glu)
4g.67753936C>ACA357054606GNRHRc.400G>T (p.Val134Leu)
4g.67753936C>GCA357054608GNRHRc.400G>C (p.Val134Leu)
4g.67753936C>TCA357054609GNRHRc.400G>A (p.Val134Met)
gnomAD v4
4g.67753937C>ACA439930678GNRHRc.399G>T (p.Val133=)
4g.67753937C=CA1465420647GNRHRc.399G= (p.Val133=)
4g.67753937C>GCA439930675GNRHRc.399G>C (p.Val133=)
4g.67753937C>TCA439930676GNRHRc.399G>A (p.Val133=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.67753938A>CCA357054611GNRHRc.398T>G (p.Val133Gly)
4g.67753938A>GCA357054613GNRHRc.398T>C (p.Val133Ala)
gnomAD v4
4g.67753938A>TCA357054614GNRHRc.398T>A (p.Val133Glu)
4g.67753939C>ACA357054615GNRHRc.397G>T (p.Val133Leu)

Number of alleles fetched